Materials Map

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (1/1 displayed)

  • 2006Large damage threshold and small electron escape depth in X-ray absorption spectroscopy of a conjugated polymer thin film56citations

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Chart of shared publication
Dipankar, Mandal
1 / 1 shared
Chua, Lay-Lay
1 / 1 shared
Gao, Xingyu
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Wee, Andrew T. S.
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Ho, Peter K. H.
1 / 2 shared
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2006

Co-Authors (by relevance)

  • Dipankar, Mandal
  • Chua, Lay-Lay
  • Gao, Xingyu
  • Wee, Andrew T. S.
  • Ho, Peter K. H.
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article

Large damage threshold and small electron escape depth in X-ray absorption spectroscopy of a conjugated polymer thin film

  • Dipankar, Mandal
  • Chua, Lay-Lay
  • Gao, Xingyu
  • Sivaramakrishnan, Sankaran
  • Wee, Andrew T. S.
  • Ho, Peter K. H.
Abstract

The information depth of near-edge X-ray absorption fine structure spectroscopy in the total electron yield mode (TEY-NEXAFS) is given by the escape depth of the TEY electrons <i>z</i><sub>TEY</sub>. This is determined by the effective ranges both of the inelastically scattered secondary electrons and of the primary excited electron before they thermalize below the vacuum level. For regioregular poly(3-hexylthiophene) (rreg-P3HT) thin films, we have measured the total electron emission efficiency to be 0.028 ± 0.005 e/ph at an incident photon energy of 320 eV. The range of the primary electron was computed using optical dielectric-loss theory to be 7.5 nm. The range of the secondary electrons was then found by modeling to be 3.0 nm. This gives <i>z</i><sub>TEY</sub> to be 2.5 nm, which is considerably less than the often-assumed value of 10 nm in the literature. It is also considerably smaller than the computed electron−electron scattering inelastic mean free path in the material, which suggests the predominance of electron−phonon scattering. Thus, TEY-NEXAFS has sufficient surface sensitivity to probe the frontier molecular layers of these organic conjugated polymers. In a second aspect of this report, the rreg-P3HT films have been characterized by in-situ core and valence photoemission spectroscopies and by ex-situ microattenuated total-reflection vibrational spectroscopy as a function of irradiation dose. No damage was observed in composition, bonding, orientation, and surface morphology under typical TEY-NEXAFS spectral acquisition conditions. For an integrated TEY that exceeds 2 × 10<sup>-</sup><sup>3</sup> C cm<sup>-</sup><sup>2</sup>, however, the material degrades via alkyl side-chain dehydrogenation to unsaturated units, cross linking, ring opening of the backbone, and sulfur extrusion. Given that secondary electrons are the dominant cause of radiation damage, this exposure threshold measured by integrated TEY should also be valid at other X-ray energies.

Topics
  • impedance spectroscopy
  • surface
  • polymer
  • theory
  • thin film
  • extrusion
  • laser emission spectroscopy
  • vibrational spectroscopy
  • near-edge X-ray absorption fine structure spectroscopy